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1.
Sensors (Basel) ; 11(9): 8485-96, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-22164087

RESUMO

This paper presents a prototype wireless remote glucose monitoring system interfaced with a ZnO nanowire arrays-based glucose sensor, glucose oxidase enzyme immobilized onto ZnO nanowires in conjunction with a Nafion® membrane coating, which can be effectively applied for the monitoring of glucose levels in diabetics. Global system for mobile communications (GSM) services like general packet radio service (GPRS) and Short Message Service (SMS) have been proven to be logical and cost effective methods for gathering data from remote locations. A communication protocol that facilitates remote data collection using SMS has been utilized for monitoring a patient's sugar levels. In this study, we demonstrate the remote monitoring of the glucose levels with existing GPRS/GSM network infra-structures using our proposed functionalized ZnO nanowire arrays sensors integrated with standard readily available mobile phones. The data can be used for centralized monitoring and other purposes. Such applications can reduce health care costs and allow caregivers to monitor and support to their patients remotely, especially those located in rural areas.


Assuntos
Glucose Oxidase/química , Glucose/análise , Nanofios , Ondas de Rádio , Óxido de Zinco/química , Microscopia Eletrônica de Varredura , Envio de Mensagens de Texto
2.
J Med Chem ; 45(18): 3813-5, 2002 Aug 29.
Artigo em Inglês | MEDLINE | ID: mdl-12190302

RESUMO

Novel antidiabetic arylsulfonamidothiazoles are presented that exert action through selective inhibition of the 11beta-hydroxysteroid dehydrogenase type 1 (11beta-HSD1) enzyme, thereby attenuating hepatic gluconeogenesis. The diethylamide derivative 2a was shown to potently inhibit human 11beta-HSD1 (IC(50) = 52 nM), whereas the N-methylpiperazinamide analogue 2b only inhibited murine 11beta-HSD1 (IC(50) = 96 nM). Both compounds showed >200-fold selectivity over human and murine 11beta-HSD2. 2b was subsequently shown to reduce glucose levels in diabetic KKA(y) mice, substantiating the 11beta-HSD1 enzyme as a target for the treatment of type 2 diabetes.


Assuntos
Hidroxiesteroide Desidrogenases/antagonistas & inibidores , Hipoglicemiantes/síntese química , Sulfonamidas/síntese química , Tiazóis/síntese química , 11-beta-Hidroxiesteroide Desidrogenase Tipo 1 , Animais , Glicemia/metabolismo , Humanos , Hipoglicemiantes/química , Hipoglicemiantes/farmacologia , Camundongos , Relação Estrutura-Atividade , Sulfonamidas/química , Sulfonamidas/farmacologia , Tiazóis/química , Tiazóis/farmacologia
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